This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
Pfizer is seeking a Manager, Medical Device Quality Assurance to lead quality oversight for MDCP programs across development and sustaining activities. You will guide risk-based decisions, ensure compliance with 21 CFR 820, ISO 13485, and ISO 14971, and work with cross-functional teams to resolve issues and strengthen processes across the product lifecycle.
You will review device investigations, support post-market activities, and translate evolving regulations into effective quality system
#J-18808-Ljbffr
Worksite address
mcpherson, KS, 67460, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.